Newborn Screening Plus Test | Lahalak Platform
An integrated screening program including cystic fibrosis, endocrine, and metabolic disorder detection, giving your baby the best possible healthy start through early and accurate diagnosis.
Scientific name: Newborn Screening Plus (Including CF)
A newborn screening program involves analyzing a blood sample taken from the baby's heel to detect a range of serious congenital disorders. This typically includes screening for congenital hypothyroidism, cystic fibrosis (CF), metabolic disorders of amino acids and organic acids, and fatty acid oxidation, as well as other conditions as determined b...
Service type
Newborn Preventive Screening
Duration
10-15 minutes
Fasting
Fasting is not required
Included Services
- Extensive examination of disorders of amino acid and organic acid metabolism and fatty acid oxidation.
- Congenital hypothyroidism (TSH) and cystic fibrosis (IRT/CF DNA) testing.
- Consult a pediatrician or metabolism specialist to interpret the overall results.
- Personal support services from Lehlek to guide you towards confirmatory tests and appropriate care if needed.
Medical Service Information
Conditions & Notices
- The child does not need to fast before the sample is taken.
- The sample should be taken at least 24 hours after the start of breastfeeding or formula feeding to ensure the accuracy of the metabolic test.
- The sample is taken by pricking the child's heel and collecting a few drops of blood on special filter paper.
- It is recommended that all newborns undergo testing regardless of the appearance of any symptoms.
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